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Items: 1 to 20 of 91

1.

A new syndrome mimicking Jaffe-Campanacci syndrome: a case report.

Sevencan A, İnan U, Köse N.

Eklem Hastalik Cerrahisi. 2013;24(1):46-8. doi: 10.5606/ehc.2013.11.

2.

Jaffe-Campanacci syndrome.

Al-Rikabi AC, Ramaswamy JC, Bhat VV.

Saudi Med J. 2005 Jan;26(1):104-6.

PMID:
15756363
3.

Jaffe-Campanacci syndrome, revisited: detailed clinical and molecular analyses determine whether patients have neurofibromatosis type 1, coincidental manifestations, or a distinct disorder.

Stewart DR, Brems H, Gomes AG, Ruppert SL, Callens T, Williams J, Claes K, Bober MB, Hachen R, Kaban LB, Li H, Lin A, McDonald M, Melancon S, Ortenberg J, Radtke HB, Samson I, Saul RA, Shen J, Siqveland E, Toler TL, van Maarle M, Wallace M, Williams M, Legius E, Messiaen L.

Genet Med. 2014 Jun;16(6):448-59. doi: 10.1038/gim.2013.163. Epub 2013 Nov 14.

PMID:
24232412
4.

Pathological fractures on both lower limbs with Jaffe-Campanacci's syndrome.

Sonar M, Isik M, Ekmekci AY, Solmaz OA.

BMJ Case Rep. 2012 Oct 19;2012. pii: bcr2012007047. doi: 10.1136/bcr-2012-007047.

5.

Is Jaffe-Campanacci syndrome just a manifestation of neurofibromatosis type 1?

Colby RS, Saul RA.

Am J Med Genet A. 2003 Nov 15;123A(1):60-3.

PMID:
14556247
6.

[Jaffe-Campanacci syndrome: report of a case].

Zhou YH, Bi LR, Wang JB, Wang YP, Orr W.

Zhonghua Bing Li Xue Za Zhi. 2011 Jun;40(6):409. Chinese. No abstract available.

PMID:
21914352
7.

[Jaffe-Campanacci syndrome. Report of a case].

Boivin C, Kerbrat JB, Michot C, Peron JM, Hemet J.

Ann Pathol. 1994;14(2):108-11. Review. French.

PMID:
8198635
8.

The diagnostic and clinical significance of café-au-lait macules.

Shah KN.

Pediatr Clin North Am. 2010 Oct;57(5):1131-53. doi: 10.1016/j.pcl.2010.07.002. Review.

PMID:
20888463
9.

Jaffe-Campanacci syndrome. A case report and review of the literature.

Hau MA, Fox EJ, Cates JM, Brigman BE, Mankin HJ.

J Bone Joint Surg Am. 2002 Apr;84-A(4):634-8. Review. No abstract available.

PMID:
11940628
10.

Multiple café au lait spots in familial patients with MAP2K2 mutation.

Takenouchi T, Shimizu A, Torii C, Kosaki R, Takahashi T, Saya H, Kosaki K.

Am J Med Genet A. 2014 Feb;164A(2):392-6. doi: 10.1002/ajmg.a.36288. Epub 2013 Dec 5. Review.

PMID:
24311457
11.

[Brown spots on the whole body: the mother has them as well. Neurofibromatosis].

Stiefelhagen P.

MMW Fortschr Med. 2013 Nov 14;155 Spec No 2:7, 35. German. No abstract available.

PMID:
24734438
12.

Multiple non-ossifying fibromas as a cause of pathological femoral fracture in Jaffe-Campanacci syndrome.

Cherix S, Bildé Y, Becce F, Letovanec I, Rüdiger HA.

BMC Musculoskelet Disord. 2014 Jun 26;15:218. doi: 10.1186/1471-2474-15-218.

13.

Multiple non-ossifying fibromata with extraskeletal anomalies: a new syndrome?

Campanacci M, Laus M, Boriani S.

J Bone Joint Surg Br. 1983 Nov;65(5):627-32.

14.

[Neurofibromatosis--easy to see, easy to overlook. Interview by Kjell Arne Bakke].

Farmen M.

Tidsskr Sykepl. 1997 Sep 16;85(15):30-3. Norwegian. No abstract available.

PMID:
9362945
15.

Short stature and growth hormone deficiency in a girl with encephalocraniocutaneous lipomatosis and Jaffe-Campanacci syndrome: a case report.

Choi EM, Jung N, Shim YJ, Choi HJ, Kim JS, Kim HS, Song KS, Lee HJ, Kim SP.

Ann Pediatr Endocrinol Metab. 2016 Dec;21(4):240-244. doi: 10.6065/apem.2016.21.4.240. Epub 2016 Dec 31.

16.

Non-ossifying fibroma, fibrous cortical defect and Jaffe-Campanacci syndrome: a biologic and clinical review.

Mankin HJ, Trahan CA, Fondren G, Mankin CJ.

Chir Organi Mov. 2009 May;93(1):1-7. doi: 10.1007/s12306-009-0016-4. Epub 2009 Apr 29. Review.

PMID:
19711155
17.

Lumbar lipomeningomyelocele associated with multiple café au lait spots: a case report.

Balasubramanian P, Srinivas CR, Arunachalam P, Thirumurthy KS, Rajkumar PR, Manuvidhya H.

Pediatr Dermatol. 2015 May-Jun;32(3):e78-81. doi: 10.1111/pde.12557. Epub 2015 Mar 19.

PMID:
25786983
18.

Deep-seated segmental neurofibromatosis without café au lait spots.

Ogose A, Hotta T, Imaizumi S, Saito H, Homma T, Takahashi HE.

Skeletal Radiol. 2000 Sep;29(9):543-7. Review.

PMID:
11000302
19.

The first case of Niikawa-Kuroki syndrome in Kazakhstan associated with café au lait spots.

Al Mosawi AJ, Fewin L.

G Ital Dermatol Venereol. 2009 Oct;144(5):613-5.

PMID:
19834439
20.

Pigmentary anomalies in the multiple lentigines syndrome: Is it distinct from LEOPARD syndrome?

Arnsmeier SL, Paller AS.

Pediatr Dermatol. 1996 Mar-Apr;13(2):100-4.

PMID:
9122064

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